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Lancet (London, England)
|
August 3, 1991
Motoneuron-disease-like disorder after ganglioside therapy
G Scarlato, E Nobile-Orazio
Acta Neuropathologica. Supplementum
|
January 1, 1981
Ophthalmoplegia plus: neuropathological and metabolic studies with a therapeutic trial in seven cases
G Pellegrini, G Scarlato, M Moggio
Journal of Neurology
|
April 23, 1976
Quantitative electromyography in the detection of the carriers in Duchenne type muscular dystrophy
G Valli, G Scarlato, M Contartese
Advances in Experimental Medicine and Biology
|
January 1, 1982
alpha-Ketoglutarate induced transamination during ischemic exercise
C Cerri, F Fici, G Scarlato
Electromyography and Clinical Neurophysiology
|
January 1, 1983
Neurophysiological tests in human botulism
G Valli, S Barbieri, G Scarlato
Journal of Neurology
|
January 1, 1980
A hereditary case of lipid storage myopathy with carnitine deficiency. Ultrastructural observation of muscle tissue in parents
G Pellegrini, G Scarlato, M Moggio
Acta Neurologica
|
March 1, 1970
[Nosography of infantile and juvenile neurogenic amyotrophias in the light of histoenzymological studies]
G Scarlato, F Cornelio, A Bollati
Journal of Neuropathology and Experimental Neurology
|
January 1, 1978
Morphologic and metabolic studies in a case of oculo-cranio-somatic neuromuscular disease
G Scarlato, G Pellegrini, A Veicsteinas
Rivista Di Patologia Nervosa E Mentale
|
May 1, 1977
[Prevention of duchenne's muscular dystrophy: methodological problems in the detection of carriers (author's transl)]
G Scarlato, G Valli, G Meola
Acta Neurologica
|
July 1, 1974
[Histoenzymological particularities in a case of neuromyotonia]
G Scarlato, R Schoenhuber, G Valli
Page
of 31
Search research articles
Search
Showing results (11-20 of 302) with videos related to
Sort By:
Page
of 31
Lancet (London, England)
|
August 3, 1991
Motoneuron-disease-like disorder after ganglioside therapy
G Scarlato, E Nobile-Orazio
Acta Neuropathologica. Supplementum
|
January 1, 1981
Ophthalmoplegia plus: neuropathological and metabolic studies with a therapeutic trial in seven cases
G Pellegrini, G Scarlato, M Moggio
Journal of Neurology
|
April 23, 1976
Quantitative electromyography in the detection of the carriers in Duchenne type muscular dystrophy
G Valli, G Scarlato, M Contartese
Advances in Experimental Medicine and Biology
|
January 1, 1982
alpha-Ketoglutarate induced transamination during ischemic exercise
C Cerri, F Fici, G Scarlato
Electromyography and Clinical Neurophysiology
|
January 1, 1983
Neurophysiological tests in human botulism
G Valli, S Barbieri, G Scarlato
Journal of Neurology
|
January 1, 1980
A hereditary case of lipid storage myopathy with carnitine deficiency. Ultrastructural observation of muscle tissue in parents
G Pellegrini, G Scarlato, M Moggio
Acta Neurologica
|
March 1, 1970
[Nosography of infantile and juvenile neurogenic amyotrophias in the light of histoenzymological studies]
G Scarlato, F Cornelio, A Bollati
Journal of Neuropathology and Experimental Neurology
|
January 1, 1978
Morphologic and metabolic studies in a case of oculo-cranio-somatic neuromuscular disease
G Scarlato, G Pellegrini, A Veicsteinas
Rivista Di Patologia Nervosa E Mentale
|
May 1, 1977
[Prevention of duchenne's muscular dystrophy: methodological problems in the detection of carriers (author's transl)]
G Scarlato, G Valli, G Meola
Acta Neurologica
|
July 1, 1974
[Histoenzymological particularities in a case of neuromyotonia]
G Scarlato, R Schoenhuber, G Valli
Page
of 31